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巴黎地区交通和郊区站点颗粒态多环芳烃、邻苯二甲酸酯和非邻苯二甲酸酯的昼夜浓度及来源。

Diurnal/nocturnal concentrations and sources of particulate-bound PAHs, OPAHs and NPAHs at traffic and suburban sites in the region of Paris (France).

机构信息

Institut National de l'Environnement industriel et des RISques (INERIS), Parc technologique Alata BP2, 60550 Verneuil en Halatte, France.

出版信息

Sci Total Environ. 2012 Oct 15;437:297-305. doi: 10.1016/j.scitotenv.2012.07.072. Epub 2012 Sep 1.

Abstract

Particulate concentrations of polycyclic aromatic compounds (PACs) including, 17 polycyclic aromatic hydrocarbons (PAHs), 9 oxygenated PAHs (OPAHs) and 18 nitrated PAHs (NPAHs) were determined at traffic and suburban sites located in the region of Paris. A 12 h sampling basis time resolution was applied in order to study their diurnal and nocturnal variations. Observed concentrations were about 10 times higher at the traffic site for all compounds and were higher during the night-time for both sites (except for NPAHs at the traffic site). No significant differences in PAH and OPAH profiles were observed at both sites whereas, for NPAHs, 1-nitropyrene (diesel source) was the most abundant at the traffic site and 2+3-nitrofluoranthene (secondary formed by gas-phase reaction) was predominant at the suburban site. The study of the specific ratio 2-nitrofluoranthene/1-nitropyrene (2-NFlt/1-NP) showed a local formation of NPAHs in gaseous phase at the suburban site. A detailed analysis showed that atmospheric humidity and rainfalls modified differently PAH and NPAH profiles, in comparison to OPAH. A difference of the scale variability of water solubility between, light (MW≤228 g mol(-1)) and heavy compounds (MW≥273 g mol(-1)), could explain these observations. The specific study of the relationships between PACs and other measured pollutants highlighted that particle resuspension could constitute a significant source of PM on the traffic site. Even if NPAH formation seemed clearly evident at the suburban site during periods characterised by high O(3) and NO(2) concentration levels, results showed also that the primary and/or secondary origins of OPAHs and NPAHs were strongly dependent on the sampling site and on sampling conditions. Finally, we conclude that higher time sampling resolutions would be helpful in investigating the atmospheric chemistry and behaviours of PACs in correlation with the local meteorological variations and the daily cycle of human activities.

摘要

在巴黎地区的交通和郊区站点,测定了多环芳烃(PAC)的颗粒浓度,包括 17 种多环芳烃(PAHs)、9 种含氧多环芳烃(OPAHs)和 18 种硝基多环芳烃(NPAHs)。采用 12 小时采样基础时间分辨率来研究它们的日变化和夜间变化。所有化合物在交通站点的观测浓度均比郊区站点高约 10 倍,且两个站点在夜间的浓度均较高(交通站点的 NPAHs 除外)。在两个站点均未观察到 PAH 和 OPAH 谱的显著差异,而对于 NPAHs,1-硝基芘(柴油源)在交通站点最丰富,2+3-硝基荧蒽(由气相反应生成的二次污染物)在郊区站点占优势。对特定比值 2-硝基荧蒽/1-硝基芘(2-NFlt/1-NP)的研究表明,在郊区站点的气相中存在 NPAHs 的局部形成。详细分析表明,与 OPAH 相比,大气湿度和降雨量对 PAH 和 NPAH 谱的影响不同。轻(MW≤228 g mol(-1)) 和重化合物(MW≥273 g mol(-1)) 之间水溶性的标度可变性的差异,可以解释这些观察结果。对 PACs 与其他测量污染物之间的关系的专门研究表明,颗粒物再悬浮可能是交通站点 PM 的一个重要来源。即使在 O3 和 NO2 浓度水平较高的时期,NPAH 的形成在郊区站点显然很明显,但结果还表明,OPAHs 和 NPAHs 的主要和/或次要来源强烈依赖于采样站点和采样条件。最后,我们得出结论,更高的时间采样分辨率将有助于研究 PACs 的大气化学和行为,与当地气象变化和人类活动的日常周期相关联。

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